FDA Device recall Z-0176-2014
Pinook Mini Massager Distributed by www.pinookusa.com
- FDA Device
- Class II
- terminated
- Published 2013-11-13
On 2013-11-13 the FDA classified a Class II recall of Pinook Mini Massager Distributed by www.pinookusa.com by Pinook Usa, citing failure to submit a premarket submission and gain approval of a medical device.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0176-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-23 |
| Published | 2013-11-13 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Pinook Usa |
| Distribution | US |
Product
Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen the abdominal muscles.
Reason
Failure to submit a premarket submission and gain approval of a medical device.
Identifiers
| code_info | ALL LOTS |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0176-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.